Isolation of polysaccharide producers and heavy metal-tolerant local rhizobial isolates

Mohammed Hamid Jasim, Raad Hassani Sultan

Abstract


Background: Rhizobia are important soil bacteria that enter into a relationship with leguminous plants and fix nitrogen symbiotically. The importance of this relation is not only for soil as a soil fertilizer but also to keep our environment without pollution.      

Methods: A Survey was conducted to collect different strains of rhizobial from different areas in Nineveh Governorate in Iraq. Isolation and biochemical tests were done under laboratory conditions. Determination of exopolysaccharide and tolerance to heavy metals was also conducted. Data obtained was recorded after cultivation and incubation of rhizobial strains.

Results: The rhizobial bacteria were isolated from the following leguminous plants: Vigna unguiculata L., Trifolium alexandrinum, Trigonella foenum-graecum L., Leucaena leucocephala L., Medicago sativa L., Phaseolus vulgaris L., Tribulus terrestris L., and Vicia faba L. Maximum exopolysaccharide production was reached at 3.76 gm/L by the isolate R. leguminosarum bv. Viciae RM25, after two days of incubation. The maximum cell dry weight was 3.50 gm/L. by the isolate E. meliloti RM5, after two days of incubation. The maximum reduction in pH was 4.80 by strain E. meliloti RM14, after two days of incubation. All the local isolated rhizobia were tolerant of nickel chloride for the studied concentrations: 100, 500, 1000, and 5000 µg/ ml. Also, we were tolerant to 100 and 500 µg/ ml of zinc sulfate and copper sulfate. All rhizobial isolates also tolerated a 1000 µg/ ml concentration of zinc sulfate.

Conclusion: Rhizobium bacteria possess several mechanisms that allow them to tolerate heavy metal exposure. These mechanisms include the expression of efflux pumps, the presence of metal-resistance plasmids, the production of EPS, and the ability to adapt to environmental factors. Further research is needed to fully understand the mechanisms behind the heavy metal tolerance in Rhizobium and to explore the potential applications of these bacteria in the bioremediation of heavy metal-polluted soils.

Keywords: Rhizobium; Isolation; Exopolysaccharide production; Heavy metal tolerance

Editorial Note: You are viewing the latest version of this article having language and SI units corrections.


Full Text:

PDF

References


Haing T, Kyaw KN, Kyi HH, Naing KM. Isolation of rhizobia from the root nodules of cow pea & black gram cultivated in Kyaungkone, Myanmar. Journal of the Myanmar Academy of Arts and Science, (2020); 18(3): 135-143.

Ghadbane M, Benderradji L, Medjekal S, Belhadj H, Daoud H. Plant growth promoting & heavy metal-tolerant rhizobia from Algeria. Euro-Mediterranean conference for environmental integration, (2021): pp 697-701.

Jach ME, Sajnaga E, Ziaja M. Utilization of legume-nodule bacterial symbiosis in phytoremediation of heavy metal-contaminated soils. Biology, (2022); 11(5): 676-689.

Lakzain A, Murphy P, Turner A, Beynon JL , Giller KE. Rhizobium leguminosarum bv. Viciae populations in soils with increasing heavy metal contamination: abundance, plasmid profiles, diversity & metal tolerance. Soil Biology & Biotechnology, (2002); 34(4): 519-529.

5.Rubio-Sanz L, Brito B, Palacios J. Analysis of metal tolerance in Rhizobium leguminosarum strains isolated from ultramafic soil. FEMS Microbiology Letters, (2018); 365(4): 1-7.

Lakzain A, Murphy P, Giller K E. Transfer and loss of naturally-occurring plasmids among isolates of Rhizobium leguminosarum bv. Viciae in heavy metal contaminated soils. Soil Biology and Biochemistry, (2007): 39(5): 1066-1077.

Thakur AK, Singh KJ. Effect of cadmium on plasmid profile of nitrogen fixing Rhizobium. Indian Journal of Plant Sciences, (2014); 4(3): 2319-3824.

Sazykin I, Khmelevtsova L, Azhogina T, Sazykina M. Heavy metals influence on the bacterial community of soils: A review. Agriculture, (2023); 13(3): 653-676.

Goyal RK, Habtewold JZ. Evaluation of legume-rhizobial symbiotic interactions beyond nitrogen fixation that help the host survival and diversification in hostile environments. Microorganisms, (2023); 11(6): 1454-1472.

Ali A, Orf H O M. Screening and increase of exopolysaccharide production by rhizobial strains, stress tolerances and its efficiency with “ in vivo “ peanut plants. Egyptian Journal of Agriculture and Research, (2022); 100(1): 11-21.

Moretto C, Castellane TCL, Leonel TF. Bioremediation of heavy metal-polluted environment by non-living cells from rhizobial isolates. Environmental Science and Pollution Research, (2022); 29(31): 46953-46967.

Vincent JM. A Manual for the Practical Study of the Root Nodule Bacteria. I. B. P. Handbook No. 15 Oxford Black well Scientific Publications. Oxford Ltd., U. K., 1970.

Mir MI, Kumar BK, Gopalakrishnan S. characterization of rhizobia isolated from leguminous plants and their impact on the growth of ICCV2 variety of chickpea (Cicer arietinum L.). Heliyon, (2021); 7(11): 8321-8334.

Ghosh AC, Basu PS. Extracellular polysaccharide production by Azorhizobium caulinodans from stem nodules of leguminous emergent hydrophyte Aeschyromene aspera. Indian Journal of Experimental Biology, (2001); 39(2): 155-159.

Duta FP, Franca FP, Lopes, LD. Optimization of culture conditions for exopolysaccharides production in Rhizobium sp. Using the response service method. Electronic Journal of Biotechnology, (2006); 9(4): 391-399.

Teresa MS, Goma-Tchimbakala J, Eckzechel NSA. Isolation and characterization of native Rhizobium strains nodulating some legumes species in South Brazzaville in Republic of Congo.Advances in Bioscience and Biotechnology, (2021); 12(01): 10-30.

Sridevi, M. & Mallaiah, K. V. Production of extra cellular polysaccharide by Rhizobium strains from root nodules of leguminous green manure crop, Sesbania sesban (L.) Merr. International Journal of Soil Science, (2007); 2(4): 308-313.

SAS Institute Inc. SAS/STAT® 9.2 Users Gide, Second Edition. Cary, N. C.: SAS Institute Inc.2009.

Qasim WS. Production of exopolysaccharide from local isolates of Rhizobium leguminosarum bv. Viciae. Mesopotomia Journal of Agriculture, (2022); 50(3): 97-107.

Breadveld NW, Zevenhuizen LPTM, Cremers HCJC, Zehnder AJB. (1993). Influence of growth conditions on production of capsular and extracellular polysaccharides by

Rhizobium leguminosarum. Antonie Van Leeuwenhoek, (1993); 64: 1-8.

Nirmala R, Aysha OS, Valli S, Reena A, Kumar PV. Production of Extracellular polysaccharides by Rhizobium species from root nodules of Vignamungo (Hepper). International Journal of Pharmaceutical & Biological Archives, (2011); 2(4): 1209-1214.

Howieson JG. Use of an organic buffer for the selection of acid tolerant Rhizobium meliloti strains. Plant and Soil, (1985); 88: 367-376.

Shen T, Jin R, Yan J, Cheng X, Zeng L, et al. (2023). Study on diversity, nitrogen-fixing capacity, and heavy metal tolerance of culturable Pongamia pinnata rhizobia in the vanadium-titanium magnetite tailings. Frontiers in Microbiology, (2023): 14: 1-12.

Liu H, Cui Y, Zhou J, Penttinen P, Liu J, et al. Nickel mine soil is a potential source for soybean plant growth promoting and heavy metal tolerant rhizobia. Peer Journal, (2022); 10: 13215-13226.

Rahal S, Chekireb D. diversity of rhizobia and non-rhizobia endophytes isolated from root nodules of Trifolium sp. growing in lead and zinc mine site Guelma Algeria. Archives of Microbiology, (2021); 203(7): 3839-3849.

Fagorzi C, Checcucci A, diCenzo GC, Debiec-Andrzejewska K, Dziewit L, Pini F, Mengoni A. Harnessing rhizobia to improve heavy-metal phytoremediation by legumes. Genes, (2018); 9(1): 542-558.

El-Aziz R, Angle JS, Chaney RL. Metal tolerance of Rhizobium italic isolated from heavy-metal contaminated soils. Soil Biology and Biochemistry, (1991); 23(8): 795-798.




DOI: http://dx.doi.org/10.62940/als.v10i4.2314

Refbacks

  • There are currently no refbacks.